Taiwan FDA registration d0fdcb1c98db251b114d0f8914a98435

Cold Photochemical Analyzer (Unsterilized)

TW: 錄秘帕斯 冷光化學分析儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·TERAMECS CO., LTD.·Registered May 30, 2014 – May 30, 2019Cancelled
Registration details
Analysis ID
d0fdcb1c98db251b114d0f8914a98435
Customs Code
DHA09401419300
Company information
Manufacturer
TERAMECS CO., LTD.
Manufacturer Country
Japan
Authorized Representative
Taiwan Fu Pharmaceutical Co., Ltd
Product details
Intended Use
Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
May 30, 2014
Expiry Date
May 30, 2019
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for Cold Photochemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d0fdcb1c98db251b114d0f8914a98435 and manufactured by TERAMECS CO., LTD.. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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